| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3804100 | 0.633 | 0.720 | 4 | 153704257 | synonymous variant | T/C | snv | 9.0E-02 | 6.7E-02 | 36 | |
| rs117026326 | 0.752 | 0.440 | 7 | 74711703 | intron variant | C/T | snv | 1.3E-02 | 10 | ||
| rs149660944 | 0.851 | 0.200 | 19 | 33772017 | missense variant | C/A;T | snv | 6.5E-05; 4.0E-03 | 5 | ||
| rs13072846 | 0.882 | 0.200 | 3 | 29402923 | intron variant | G/A | snv | 0.28 | 3 | ||
| rs13079920 | 0.882 | 0.200 | 3 | 29404440 | intron variant | G/A;T | snv | 3 | |||
| rs5743705 | 0.882 | 0.200 | 4 | 153705028 | synonymous variant | T/C | snv | 1.4E-02 | 5.1E-03 | 3 |